Common Milgamma Side Effects

The most commonly reported Milgamma side effects (click to view or check a box to report):

Eye Disorder (1)
Memory Impairment (1)
Mental Status Changes (1)
Disturbance In Attention (1)
Disorientation (1)
Condition Aggravated (1)
Confusional State (1)
Apathy (1)

If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Milgamma Side Effects Reported to FDA

Milgamma Side Effect Report#8403655-X
Condition Aggravated, Memory Impairment, Confusional State, Disorientation, Mental Status Changes, Apathy, Disturbance In Attention
This is a report of a female patient (weight: NA) from Czech Republic, suffering from the following health symptoms/conditions: vitamin supplementation,niemann-pick disease, who was treated with Milgamma (dosage: Unk, start time:
Apr 10, 2012), combined with:
  • Zavesca (100 Mg, Tid)
  • Zavesca (100 Mg, Tid)
  • Asentra (Unk)
  • Cyanocobalamin
  • Thiamine Hcl
  • Zavesca (100 Mg, Tid)
and developed a serious reaction and side effect(s): Condition Aggravated, Memory Impairment, Confusional State, Disorientation, Mental Status Changes, Apathy, Disturbance In Attention after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Milgamma treatment in female patients, resulting in Condition Aggravated side effect.
Milgamma Side Effect Report#7777619-3
Eye Disorder
This report suggests a potential Milgamma Eye Disorder side effect(s) that can have serious consequences. A male patient (weight: NA) from Russian Federation was diagnosed with the following symptoms/conditions: tonsillitis and used Milgamma (dosage: Unk) starting
Apr 28, 2011. After starting Milgamma the patient began experiencing various side effects, including: Eye DisorderAdditional drugs used concurrently:
  • Alemtuzumab (12 Mg, Qd)
  • Alemtuzumab (12 Mg, Qd)
  • Hexetidine (Unk)
  • Levothyroxine Sodium (100 Mcg, Qd)
  • Amoxicillin And Clavulanate Potassium (1.2 G, Bid)
  • Alemtuzumab (12 Mg, Qd)
  • Ciprofloxacin (Unk)
  • Ketoprofen (50 Mg, Once)
The patient was hospitalized. Although Milgamma demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Eye Disorder, may still occur.

The appearance of Milgamma on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.

What are common Milgamma Side Effects for Women?

Women Side Effects Reports
Apathy 1
Condition Aggravated 1
Confusional State 1
Disorientation 1
Disturbance In Attention 1
Memory Impairment 1
Mental Status Changes 1

What are common Milgamma Side Effects for Men?

Men Side Effects Reports
Eye Disorder 1

Track Your Side Effects

Note Your Observations

It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

    You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

    Milgamma reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
    FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

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    More About Milgamma

    Side Effects reported to FDA: 2

    Milgamma safety alerts: No

    Reported hospitalizations: 1

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